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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1386629Generated: October 30, 2026

Ethyl bromoacetate → HCID 15550516, compound

https://huagongshe.com/reaction/1386629

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
ReactantSodium hydrideHCID 24758—
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 15550515HCID 15550515—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 15550516HCID 15550516—

Reaction Steps

The compound (5.13 g) of Example 1 was dissolved into DMF (70 ml) and, after adding sodium hydride (1.00 g), the mixture was stirred for 1 hour at room temperature. This was cooled in ice bath and ethyl 2-bromoacetate (2.77 ml) was added. After stirring for 18 hours until the temperature rose to room temperature, saturated aqueous solution of ammonium chloride was added and diluted with water, which was extracted with ether. After the organic layer was washed with water and with saturated brine and dried over anhydrous sodium sulfate, solvent was distilled off under reduced pressure. The residue was purified by means of silica gel column chromatography (developing solvent, ethyl acetate:n-hexane=1:2) to obtain aimed product (4.63 g) as a yellow oily product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06265577B1
Source datasetuspto-grants-2001_07
ORD IDord-98a97435e27e4f06a22a2bd6d132a701
Source noteuspto-grants-2001_07